A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387775



Internal ID21045328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:69944497..69944970hg38UCSC Ensembl
chr4:70810215..70810688hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38474
hg19474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18119047
Samples
Known GenesCSN1S1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387775
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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